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The politics of precaution : an eco-political investigation of agricultural gene technology policy in Australia, 1992-2000 /Risely, Melissa. January 2003 (has links) (PDF)
Thesis (Ph.D.)--University of Adelaide, Dept. of Environmental Studies, 2003. / Bibliography: leaves 281-330.
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Die Einführung der grünen Gentechnik als diskursive Konstruktion /Oberthür, Jörg. January 2008 (has links)
Thesis (doctoral)--Universität, Jena, 2006. / Includes bibliographical references (p. 287-295).
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Development of Y-STR genotyping systems suitable for sexual assault cases in South Africa /Cloete, Kevin Wesley. January 2010 (has links) (PDF)
Thesis (M.Sc) -- University of the Western Cape, 2010. / Includes bibliographical references (leaves 79-88).
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The potential role of the genetics associate in the delivery of genetic services to families living in rural communitiesWilliams, Janet Larson. January 1979 (has links)
Thesis (M.S.)--University of Wisconsin--Madison. / Typescript. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 41-43).
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Local knowledge and the social dimensions of risk : the case of animal biopharming in New Zealand : a thesis submitted in fulfilment of the requirements for the Degree of Master of Arts in Political Science at the University of Canterbury /Shamy, David Stephen. January 2006 (has links)
Thesis (M.A.)--University of Canterbury, 2006. / Typescript (photocopy). Includes bibliographical references (leaves 132-144). Also available via the World Wide Web.
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PTD : a populus trichocarpa gene with homology to floral homeotic transcription factorsSheppard, Lorraine Anna 01 April 1997 (has links)
Graduation date: 1997
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The ethics of genomic technologyFreethy, Randy J. January 2005 (has links)
Thesis (Th. M.)--Dallas Theological Seminary, 2005. / Includes bibliographical references (leaves [61-65]).
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Les enjeux du génie génétique : articulation philosophique et étique des modifications génétiques de la nature /Warzeszak, Stanislaw. January 1900 (has links)
Thesis (doctoral). / At head ot title: Pontificia Universitas Santae Crucis, Facultas philosophiae." Includes bibliographical references (p. 477-510).
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The ethics of genomic technologyFreethy, Randy J. January 2005 (has links)
Thesis (Th.M.)--Dallas Theological Seminary, 2005. / Includes bibliographical references (leaves [61-65]).
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A NOVEL GENE TRANSFER SYSTEM FOR MAMMALIAN CELLS.SLILATY, STEVE N. January 1983 (has links)
Productive infection of mouse cells with polyoma virus yields mainly two types of particles: Complete virions and empty capsids. Empty polyoma capsids have been shown to be capable of interacting with DNA, in vitro, to form what has been referred to as polyoma-like particles (PLP). The particles are stable in high concentrations of salt and contain DNA protected by the capsid against the action of pancreatic DNase. The development of PLP into a gene transfer vehicle is the subject of the investigations described in the present dissertation. The approach has been to first, characterize the process of PLP formation and second, determine whether the genetic information contained in a specific DNA fragment and assembled into PLP in vitro can be transferred to cells and subsequently be expressed. In terms of PLP characteristics, the experimental results described in this dissertation show that the DNA extracted from PLP is heterogeneous in size. It has a mean molecular weight of 1.2 x 10⁶ with a standard deviation of ±0.5 x 10⁶. In addition, analysis of PLP DNA with restriction endonucleases revealed that a specific primary sequence or higher order structure is not required for PLP formation. Either linear, circular or supercoiled polyoma DNA, as well as, single-stranded DNA, rRNA and the synthetic homopolymers poly(dA).poly(dT) and poly(dG).poly(dC) can be used for PLP formation. Transfer of genetic information by PLP has been accomplished by using a restriction fragment containing the transforming sequences of polyoma DNA as a model gene. This fragment of polyoma DNA, which consists of 1,831 base pairs (approximately 1.2 x 10⁶ daltons) and extends clockwise from the BclI site to the EcoRI site on the conventional polyoma map, causes the induction of the transformed phenotype in rat cells grown in culture. Infection of rat F111 cells by PLP, containing this DNA fragment, results in DNA-mediated oncogenic transformation of the cells as indicated by the formation of dense foci. This gene transfer activity of PLP is shown to be 50 to 150 times more efficient than the widely used calcium phosphate coprecipitation method of introducing DNA into mammalian cells.
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